Supercritical fluid chromatography system

ABSTRACT

Provided is a supercritical fluid chromatography system, and components comprising such a system, including one or more of a supercritical fluid chiller, a supercritical fluid pressure-equalizing vessel, and a supercritical fluid cyclonic separator. The supercritical fluid chiller and the use of the chiller allow efficient and consistent pumping of liquid-phase gases employing off-the-shelf HPLC pumps in the supercritical chromatography system using liquid-phase gas mobile phase. The pressure equalizing vessel allows the use of off the shelf HPLC column cartridges in the supercritical chromatography system. The cyclonic separator efficiently and effectively allows for separation of sample molecules from a liquid phase or gas phase stream of a supercritical fluid.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is the U.S. national phase under 35 U.S.C. § 371 ofIntl. Appl. No. PCT/US2015/044306, filed on Aug. 7, 2015, which claimsthe benefit under 35 U.S.C. § 119(e) of U.S. Provisional Application No.62/039,066, filed on Aug. 19, 2014; U.S. Provisional Application No.62/039,074, filed on Aug. 19, 2014; and U.S. Provisional Application No.62/039,083, filed on Aug. 19, 2014, all of which are incorporated hereinby reference in their entireties for all purposes.

FIELD

Provided is a supercritical fluid chromatography system, and componentscomprising such a system, including one or more of a supercritical fluidchiller, a supercritical fluid pressure-equalizing vessel, and asupercritical fluid cyclonic separator.

BACKGROUND

Traditional flash chromatography is a chromatographic separationtechnique that is used to separate organic reaction mixtures to allowthe organic chemist to crudely purify the reaction products and then usethese purified products to move on to the next step of an organicsynthesis. A typical pharmaceutical synthesis has many reaction steps toget from starting materials to a final product where each of thesereaction products needs to be purified before moving on to the nextsynthetic step. The traditional flash chromatography unit employsmultiple organic solvent pumps (200 psi and 200 mls/min maximumoperation pressure and flow rate for a traditional flash chromatographyunit), a sample injection assembly where a chemist would inject thecrude reaction mix for separation, a separation column in the form of acartridge loaded with a silica or modified silica gel, a UV-VIS detector(or other form of sample detection) to detect and allow for collectionof the various fractions of the reaction mix exiting the column, and acollection tray to collect the various fractions of the reaction mixtureproducts.

Traditional flash chromatography uses large amounts of organic solvents(for example, Hexanes, Methylene Chloride, Carbon Tetra Chloride,Acetonitrile, and Chloroform) to elucidate a separation. These solventsare typically 80-90% of the flow stream through the separation column.

In the past, we have worked on a supercritical carbon dioxide prechillersystem that included a waterless refrigeration system to supplysubcooling of liquefied carbon dioxide prior to flowing into apiston-style positive displacement pump.

Since this device was created, it has undergone testing with a pumpmeant to supply high pressure carbon dioxide (e.g. >100 bar) to asupercritical carbon dioxide (scCO2) extraction system. Despite multipleattempts to improve the mechanical behavior of the pump, the system massflow rates were never proportionate to pump speed. This was indicativeof cavitation effects in the flow system comprised of duplex pump heads,each comprised of an inlet check valve, compression piston, and outletcheck valve. We made multiple attempts to characterize the system as afunction of inlet pressure and temperature. Despite significant effortto characterize the behavior, the pump performance was not repeatable.Moreover, all attempts at linearization via compensation failed.

In all cases, the inlet CO2 temperature was reduced to between 2° C. and5° C. using the waterless refrigeration system. This was readily withinthe range of single stage compressor.

SUMMARY

Chiller or Pre-Chiller

In one aspect, provided is a chiller. In some embodiments, the chillercomprises:

a) a first refrigerant circuit, comprising:

-   -   i) a first compressor that pumps refrigerant through the first        refrigerant circuit;    -   ii) a first tube-in-tube heat exchanger in fluid communication        with the first compressor, wherein the first tube-in-tube heat        exchanger comprises an inner lumen and an outer lumen that        surrounds the inner lumen, wherein the refrigerant flows through        the outer lumen;

b) a cryogenic refrigerant circuit in thermodynamic communication withthe first refrigerant circuit, the cryogenic refrigerant circuitcomprising:

-   -   i) a second compressor that pumps cryogenic refrigerant through        the cryogenic refrigerant circuit;    -   ii) the first tube-in-tube heat exchanger in fluid communication        with the second compressor; wherein the cryogenic refrigerant        flows through the inner lumen;    -   iii) a second tube-in-tube heat exchanger in fluid communication        with the first tube-in-tube heat exchanger; wherein the second        tube-in-tube heat exchanger comprises an inner lumen and an        outer lumen that surrounds the inner lumen, wherein the        cryogenic refrigerant flows through the outer lumen and wherein        liquefied gas or supercritical gas flows through the inner        lumen;

wherein the chiller does not comprise an intervening medium thatmediates heat exchange between the first refrigerant circuit and thecryogenic refrigerant circuit and wherein the liquefied gas orsupercritical gas exiting the inner lumen of the second tube-in-tubeheat exchanger is chilled. In varying embodiments, the output liquefiedgas or supercritical gas is chilled at least about 35° C. lower than theinput liquefied gas or supercritical gas. In varying embodiments, therefrigerant is selected from the group consisting of R-11, R-12, R-22,R-32, R-114, R-115, R-123, R-124, R-125, R-134A, R-142b, R-143a, R-152a,R-290, R-401A, R-401B, R-404A, R-407C, R 410A, R-409A, R-414B, R-416A,R-422B, R-422D, R-500, R-502, R-507, R-600 and mixtures thereof. Invarying embodiments, the cryogenic refrigerant is selected from thegroup consisting of R-12, R-13, R-22, R-23, R-32, R-115, R 116, R-124,R-125, R-134A, R-142b, R-143a, R-152a, R-218, R-290, R-218, R-401A, R401B, R-402A, R-402B, R-403B, R-404A, R-408A, R-409A, R-410A, R-414B,R-416A, R-422B, R-407A, R-407C, R-408A, R-409A, R-414B, R-422A, R-422B,R-422C, R-422D, R-500, R-502, R-503, R-508B, R-507, R-508B, R-600a andmixtures thereof. In varying embodiments, the first refrigerant circuitfurther comprises in fluid communication with the first compressor andthe first tube-in-tube heat exchanger: iii) a first expansion valve; andiv) a liquid to air heat exchanger. In varying embodiments, thecryogenic refrigerant circuit further comprises in fluid communicationwith the second compressor, the first tube-in-tube heat exchanger andthe second tube-in-tube heat exchanger: iv) a second expansion valve. Invarying embodiments, the chiller comprises a configuration as depictedin FIGS. 3A-3B.

In another aspect, provided are methods of supplying a liquid-phase gasto a liquefied gas or supercritical gas extraction system. In someembodiments, the methods comprise:

a) subcooling the liquid-phase gas to a temperature of −10° C. or lower;

b) pumping the subcooled liquid-phase gas into a chamber configured forextraction with liquefied gas or supercritical gas extraction, wherebythe pumping mass flow rate of the subcooled liquid phase gas isrepeatable and proportionate to pump speed. In varying embodiments, thesubcooling is performed using a chiller as described above and herein.In varying embodiments, the liquefied gas or supercritical gas isselected from the group consisting of carbon dioxide, n-butane,n-propane, isobutane, dimethyl ether, and mixtures thereof. In varyingembodiments, the liquefied gas or supercritical gas is CO2. In varyingembodiments, the pumping step employs a positive displacement pump. Invarying embodiments, the positive displacement pump is an unmodifiedhigh performance liquid chromatography (HPLC) pump. In varyingembodiments, the system further comprises a post-pump heater downstreamof and in fluid communication with the pump, wherein the post-pumpheater heats the liquefied gas or supercritical gas up to an operationaltemperature. In varying embodiments, the liquefied carbon dioxide issubcooled to a temperature in the range of about −10° C. to about −40°C. In varying embodiments, the liquefied carbon dioxide is subcooled toa temperature in the range of about −20° C. to about −40° C. In varyingembodiments, the subcooling of the liquified gas is performed employinga 2-stage refrigerant-on-refrigerant chiller system. In varyingembodiments, the pumping step employs a pump comprising at least onepump head and the method does not comprise separately cooling the atleast one pump head. In varying embodiments, the liquefied gas orsupercritical gas is pressurized to at least about 145 psi (at leastabout 10 bar).

In a further aspect, provided is a system comprising a chiller asdescribed above and herein. In some embodiments, the system comprises:

a) a tank comprising a gas stored at saturated conditions and a liquidwithdrawal means;

b) a chiller downstream of and in fluid communication with the tank,wherein the chiller subcools the gas to a temperature of −10° C. orlower;

c) a pump downstream of and in fluid communication with the tank and thechiller and a chamber configured for liquefied gas or supercritical gasextraction, wherein the pump comprises the gas at a temperature of −10°C. or lower; wherein the mass flow rate of the subcooled liquid phasegas through the pump is repeatable and proportionate to pump speed. Insome embodiments, the gas is selected from the group consisting ofcarbon dioxide, n-butane, n-propane, isobutane, dimethyl ether, andmixtures thereof. In some embodiments, the pump is a positivedisplacement pump. In some embodiments, the positive displacement pumpis an unmodified high performance liquid chromatography (HPLC) pump.

In various embodiments, the system further comprises a cyclonicseparator comprising:

a) a cyclone body comprising an inner surface, an outer circumference, atop outlet, a tangential inlet and a bottom outlet, wherein the innersurface comprises a top portion, a middle portion and a bottom portion,wherein:

-   -   i) the top portion of the inner surface comprises screw threads;    -   ii) the middle portion of the inner surface is cylindrical;    -   iii) the bottom portion of the inner surface comprises a funnel,        wherein the funnel has an angle in the range of about 30° to        about 60°; and wherein the ratio of the diameter of the outer        circumference to the inner diameter of the mid-height of the        funnel is in the range of about 3 to about 4; and

b) a cap comprising a scintered filter and screw threads, wherein thescrew threads of the cap interlock with the screw threads on the innersurface of the top portion of the cyclone body, wherein the cyclonicseparator can withstand pressures of at least about 1000 psi, andwherein the body is in fluid communication with the cap. In varyingembodiments, the bottom outlet of the body of the cyclonic separator isattached to a collection container, wherein the body is in fluidcommunication with the collection container. In varying embodiments, thecyclonic separator can withstand pressures of up to about 2000 psi. Invarying embodiments, the cyclonic separator can withstand pressures ofup to about 1500 psi. In varying embodiments, the thickness of themiddle portion and the bottom portion of the cyclone body is at leastabout 0.30 inches. In varying embodiments, the cyclone body is made of amaterial selected from the group consisting of: stainless steel andtitanium. In varying embodiments, the stainless steel comprises anaustenitic nickel-chromium-based alloy or a martensiticnickel-chromium-based alloy. In varying embodiments, the stainless steelcomprises less than about 0.1 wt. % carbon. In varying embodiments, thestainless steel comprises at least a 30,000 psi yield strength. Invarying embodiments, the stainless steel is selected from the groupconsisting of American Iron and Steel Institute (AISI) TYPE 304 SS, AISITYPE 316L, INCONEL® alloy 625, INCONEL® alloy 718, AK Steel 17-4 PH®,HASTELLOY® C-22 and HASTELLOY® C 276. In varying embodiments, thestainless steel is a nickel-chromium superalloy selected from the groupconsisting of INCONEL® alloy 625, INCONEL® alloy 718, AK Steel 17-4 PH®,HASTELLOY® C-22 and HASTELLOY® C 276. In varying embodiments, the innersurface of the cyclone body is configured to induce or guide a conicalcyclone of fluid flowing in from the tangential inlet. In varyingembodiments, the inner surface of the cyclone body does not comprise afilter or a porous surface. In varying embodiments, the inner surface ofthe cyclone body does not comprise one or more baffles. In varyingembodiments, the cyclone body does not comprise multiple inlets. Invarying embodiments, the sintered filter within the cap comprises a G-5porosity grade (1-16 microns pore size). In varying embodiments, thefunnel has an angle of about 40°; and wherein the ratio of the diameterof the outer circumference to the inner diameter of the mid-height ofthe funnel is about 3.5. In varying embodiments, the bottom outletremains open. In varying embodiments, the cyclonic separator is asdepicted in any one of FIGS. 13 to 17. In varying embodiments, thesystem comprises 2 to 8 cyclonic separators, e.g., 2, 3, 4, 5, 6, 7 or 8cyclonic separators. In varying embodiments, the interior of thecyclonic separator is in fluid connection with atmospheric pressure.

In varying embodiments, the system further comprises a pressureequalizing vessel downstream of and in fluid communication with thechiller and the pump and upstream of and in fluid communication with thecyclonic separator, the pressure equalizing vessel comprising:

i) an inner chromatography column comprising stationary phase media; and

ii) an outer column that cylindrically surrounds the length of the innercolumn, wherein the interspace between the inner diameter of the outercolumn and the outer diameter of the inner chromatography columncomprises a width of at least 1 mm, wherein the outer column withstandspressures of at least about 500 psi (about 35 bar), and wherein no partof the inner column is exposed to full internal pressure withoutbalancing external equalizing pressure. In varying embodiments, theinterspace between the inner diameter of the outer column and the outerdiameter of the inner chromatography column is filled with asupercritical fluid. In varying embodiments, the inner column and theouter column can be concurrently filled with supercritical fluid under apressure in the range of about 500 psi (about 35 bar) to about 20,000psi (about 1380 bar). In varying embodiments, the inner column and theouter column can be concurrently filled with supercritical fluid under apressure in the range of at least about 5076 psi (at least about 350bar). In varying embodiments, the pressure differential across the innercolumn from top to bottom is less than the pressure rating of the innercolumn. In varying embodiments, the pressure differential between theinternal space of the inner column and the interspace is at or less thanabout 200 psi (about 14 bar). In varying embodiments, the pressurewithin the interspace is higher than the pressure within the internalspace of the inner column. In varying embodiments, the inner columncomprises an inlet end and an outlet end and the pressure at the inletend is substantially the same as the pressure at the outlet end. Invarying embodiments, the inner column is an off-the-shelf columncompatible for use in a flash chromatography system. In varyingembodiments, the inner column comprises a size in the range of fromabout 4 grams to about 350 grams stationary phase media. In varyingembodiments, the inner column comprises a diameter in the range of about0.5 inches to about 3.5 inches and a column length in the range fromabout 3.5 inches to about 11 inches. In varying embodiments, thestationary phase comprises an average particle size in the range ofabout 10 to about 100 microns. In varying embodiments, the vesselcomprises an inlet adaptor which fits to a female slip or luer-lockconnector. In varying embodiments, the vessel comprises an outletadaptor which fits to a male slip or luer-lock connector. In varyingembodiments, the outlet adaptor comprises an O ring that seals aroundthe male slip or luer-lock connector. In varying embodiments, the innercolumn comprises an inlet end and an outlet end, wherein neither theinlet end nor the outlet end of the inner column comprises a perforatedstopper. In varying embodiments, the interspace comprises a single inletand no outlet or vent. In varying embodiments, the pressure equalizingcolumn is as depicted in FIGS. 11 and 12.

In varying embodiments, the liquefied gas or supercritical gas is CO2.In varying embodiments, the liquefied gas or supercritical gas ispressurized to at least about 145 psi (10 bar). In varying embodiments,the flow of the supercritical solvent through the system is in the rangeof about 10 ml/min, e.g., at least about 15 ml/min, 20 ml/min, 25ml/min, 30 ml/min, 35 ml/min, 40 ml/min, 45 ml/min, or 50 ml/min, toabout 300 ml/min. In varying embodiments, the system further pumps aco-solvent. In some embodiments, the co-solvent comprises an alcohol of3 or fewer carbon atoms (e.g., methanol, ethanol, propanol, isopropanol)or an acetate of 3 or fewer carbon atoms (e.g., methyl acetate, ethylacetate, propyl acetate), or mixtures thereof. In varying embodiments,the system is as depicted in FIG. 1.

In another aspect, provided are methods of performing high pressureseparation and/or extraction procedures using a flash chromatographysystem. In some embodiments, the methods comprise inputting a stream ofgas phase supercritical fluid comprising molecules into a chiller asdescribed above and herein.

Pressure Equalizing Vessel

In one aspect, provided is a pressure equalizing chromatography vesselcomprising:

i) an inner chromatography column comprising stationary phase media; and

ii) an outer column that cylindrically surrounds the length of the innercolumn, wherein the interspace between the inner diameter of the outercolumn and the outer diameter of the inner chromatography columncomprises a width of at least 1 mm, wherein the outer column withstandspressures of at least about 500 psi (about 35 bar), and wherein no partof the inner column is exposed to full internal pressure withoutbalancing external equalizing pressure. In varying embodiments, theinterspace between the inner diameter of the outer column and the outerdiameter of the inner chromatography column is filled with asupercritical fluid. In varying embodiments, the inner column and theouter column can be concurrently filled with supercritical fluid under apressure in the range of about 500 psi (about 35 bar) to about 20,000psi (about 1380 bar). In varying embodiments, the inner column and theouter column can be concurrently filled with supercritical fluid under apressure of at least about 5076 psi (at least about 350 bar). In varyingembodiments, the pressure differential across the inner column from topto bottom is less than the pressure rating for the inner column. Invarying embodiments, the pressure differential between the internalspace of the inner column and the interspace is at or less than about200 psi (about 14 bar). In varying embodiments, the pressure within theinterspace is higher than the pressure within the internal space of theinner column. In varying embodiments, the inner column comprises aninlet end and an outlet end and the pressure at the inlet end issubstantially the same as the pressure at the outlet end. In varyingembodiments, the inner column is an off-the-shelf column compatible foruse in a flash chromatography system. In varying embodiments, the innercolumn comprises a size in the range of from about 4 grams to about 350grams stationary phase media. In varying embodiments, the inner columncomprises a diameter in the range of about 0.5 inches to about 3.5inches and a column length in the range from about 3.5 inches to about11 inches. In varying embodiments, the stationary phase comprises anaverage particle size in the range of about 10 to about 100 microns. Invarying embodiments, the vessel comprises an inlet adaptor which fits toa female slip or luer-lock connector. In varying embodiments, the vesselcomprises an outlet adaptor which fits to a male slip or luer-lockconnector. In varying embodiments, the outlet adaptor comprises anO-ring that seals around the male slip or luer-lock connector. Invarying embodiments, the inner column comprises an inlet end and anoutlet end, wherein neither the inlet end nor the outlet end of theinner column comprises a perforated stopper. In varying embodiments, theinterspace comprises a single inlet and no outlet or vent. In varyingembodiments, the pressure equalizing column is as depicted in FIGS. 11and 12.

In another aspect, provided is a chromatography system comprising thepressure equalizing vessel as described above and herein, wherein thesystem is pressurized and pumps a supercritical solvent. In someembodiments, the system further comprises a supercritical solvent pumpupstream of and in fluid communication with the pressure equalizingvessel and a chiller upstream of and in fluid communication with thepump, wherein the chiller reduces the temperature of the supercriticalsolvent to about −5° C. or lower, e.g., about −10° C., −15° C., −20° C.,−25° C., or lower. In some embodiments, the chiller comprises:

a) a first refrigerant circuit, comprising:

-   -   i) a first compressor that pumps refrigerant through the first        refrigerant circuit;    -   ii) a first tube-in-tube heat exchanger in fluid communication        with the first compressor, wherein the first tube-in-tube heat        exchanger comprises an inner lumen and an outer lumen that        surrounds the inner lumen, wherein the refrigerant flows through        the outer lumen;

b) a cryogenic refrigerant circuit in thermodynamic communication withthe first refrigerant circuit, the cryogenic refrigerant circuitcomprising:

-   -   i) a second compressor that pumps cryogenic refrigerant through        the cryogenic refrigerant circuit;    -   ii) the first tube-in-tube heat exchanger in fluid communication        with the second compressor; wherein the cryogenic refrigerant        flows through the inner lumen;    -   iii) a second tube-in-tube heat exchanger in fluid communication        with the first tube-in-tube heat exchanger; wherein the second        tube-in-tube heat exchanger comprises an inner lumen and an        outer lumen that surrounds the inner lumen, wherein the        cryogenic refrigerant flows through the outer lumen and wherein        liquefied gas or supercritical gas flows through the inner        lumen;

wherein the chiller does not comprise an intervening medium thatmediates heat exchange between the first refrigerant circuit and thecryogenic refrigerant circuit and wherein the liquefied gas orsupercritical gas exiting the inner lumen of the second tube-in-tubeheat exchanger is chilled. In varying embodiments, the output liquefiedgas or supercritical gas is chilled at least about 35° C. lower than theinput liquefied gas or supercritical gas. In varying embodiments, therefrigerant is selected from the group consisting of R-11, R-12, R-22,R-32, R-114, R-115, R-123, R-124, R-125, R-134A, R-142b, R-143a, R-152a,R-290, R-401A, R-401B, R-404A, R-407C, R 410A, R-409A, R-414B, R-416A,R-422B, R-422D, R-500, R-502, R-507, R-600 and mixtures thereof. Invarying embodiments, the cryogenic refrigerant is selected from thegroup consisting of R-12, R-13, R-22, R-23, R-32, R-115, R 116, R-124,R-125, R-134A, R-142b, R-143a, R-152a, R-218, R-290, R-218, R-401A, R401B, R-402A, R-402B, R-403B, R-404A, R-408A, R-409A, R-410A, R-414B,R-416A, R-422B, R-407A, R-407C, R-408A, R-409A, R-414B, R-422A, R-422B,R-422C, R-422D, R-500, R-502, R-503, R-508B, R-507, R-508B, R-600a andmixtures thereof. In varying embodiments, the first refrigerant circuitfurther comprises in fluid communication with the first compressor andthe first tube-in-tube heat exchanger: iii) a first expansion valve; andiv) a liquid to air heat exchanger. In varying embodiments, thecryogenic refrigerant circuit further comprises in fluid communicationwith the second compressor, the first tube-in-tube heat exchanger andthe second tube-in-tube heat exchanger: iv) a second expansion valve. Invarying embodiments, the chiller comprises a configuration as depictedin FIGS. 3A-3B. In some embodiments, the system comprises:

a) a tank comprising a gas stored at saturated conditions and a liquidwithdrawal means;

b) a chiller in fluid communication with the tank, wherein the chillersubcools the gas to a temperature of −10° C. or lower;

c) a pump in fluid communication with the tank and a chamber configuredfor liquefied gas or supercritical gas extraction, wherein the pumpcomprises the gas at a temperature of −10° C. or lower; wherein the massflow rate of the subcooled liquid phase gas through the pump isrepeatable and proportionate to pump speed. In some embodiments, the gasis selected from the group consisting of carbon dioxide, n-butane,n-propane, isobutane, dimethyl ether, and mixtures thereof. In someembodiments, the pump is a positive displacement pump. In someembodiments, the positive displacement pump is an unmodified highperformance liquid chromatography (HPLC) pump. In varying embodiments,the system further comprises a post-pump heater downstream of and influid communication with the pump, wherein the post-pump heater heatsthe liquefied gas or supercritical gas up to an operational temperature.

In varying embodiments, the supercritical fluid is CO2. In varyingembodiments, the flow of the supercritical solvent through the system isin the range of about 10 ml/min, e.g., at least about 15 ml/min, 20ml/min, 25 ml/min, 30 ml/min, 35 ml/min, 40 ml/min, 45 ml/min, or 50ml/min, to about 300 ml/min. In varying embodiments, the system furtherpumps a co-solvent. In some embodiments, the co-solvent comprises analcohol of 3 or fewer carbon atoms (e.g., methanol, ethanol, propanol,isopropanol) or an acetate of 3 or fewer carbon atoms (e.g., methylacetate, ethyl acetate, propyl acetate), or mixtures thereof. In varyingembodiments, the system is as depicted in FIG. 1.

In varying embodiments, the system further comprises a cyclonicseparator downstream of and in fluid communication with the pressureequalizing vessel, the cyclonic separator comprising:

a) a cyclone body comprising an inner surface, an outer circumference, atop outlet, a tangential inlet and a bottom outlet, wherein the innersurface comprises a top portion, a middle portion and a bottom portion,wherein:

i) the top portion of the inner surface comprises screw threads;

ii) the middle portion of the inner surface is cylindrical;

iii) the bottom portion of the inner surface comprises a funnel, whereinthe funnel has an angle in the range of about 30° to about 60°; andwherein the ratio of the diameter of the outer circumference to theinner diameter of the mid-height of the funnel is in the range of about3 to about 4; and

b) a cap comprising a sintered filter and screw threads, wherein thescrew threads of the cap interlock with the screw threads on the innersurface of the top portion of the cyclone body, wherein the cyclonicseparator can withstand pressures of at least about 1000 psi, andwherein the body is in fluid communication with the cap. In varyingembodiments, the bottom outlet of the body is attached to a collectioncontainer, wherein the body is in fluid communication with thecollection container. In some embodiments, the cyclonic separator canwithstand pressures of up to about 10,000 psi, e.g, up to about 5000psi, e.g., up to about 2000 psi, e.g., up to about 1900 psi, 1800 psi,1700 psi, 1600 psi, or 1500 psi. In varying embodiments, the thicknessof the middle portion and the bottom portion of the cyclone body is atleast about 0.30 inches, e.g., at least about 0.31, 0.32, 0.33, 0.34,0.35, 0.36, 0.37, 0.375, 0.38, 0.39, 0.40 inches. In varyingembodiments, the cyclone body is made of a material selected from thegroup consisting of: stainless steel and titanium. In varyingembodiments, the stainless steel comprises an austeniticnickel-chromium-based alloy or a martensitic nickel-chromium-basedalloy. In varying embodiments, the stainless steel comprises less thanabout 0.1 wt. % carbon. In varying embodiments, the stainless steelcomprises at least a 30,000 psi yield strength. In varying embodiments,the stainless steel is selected from the group consisting of AmericanIron and Steel Institute (AISI) TYPE 304 SS, AISI TYPE 316L, INCONEL®alloy 625, INCONEL® alloy 718, AK Steel 17-4 PH®, HASTELLOY® C-22 andHASTELLOY® C-276. In varying embodiments, the stainless steel is anickel-chromium superalloy selected from the group consisting ofINCONEL® alloy 625, INCONEL® alloy 718, HASTELLOY® C-22 and HASTELLOY®C-276. In some embodiments, the inner surface of the cyclone body isconfigured to induce or guide a conical cyclone of fluid flowing in fromthe tangential inlet. In varying embodiments, the inner surface of thecyclone body does not comprise a filter or a porous surface. In varyingembodiments, the inner surface of the cyclone body does not comprise oneor more baffles. In some embodiments, the cyclone body does not comprisemultiple inlets. In some embodiments, the sintered filter within the capcomprises a G-5 porosity grade (1-16 microns pore size). In someembodiments, the funnel has an angle of about 40′; and the ratio of thediameter of the outer circumference to the inner diameter of themid-height of the funnel is about 3.5. In varying embodiments, thebottom outlet remains open. In some embodiments, the cyclonic separatoris as depicted in any one of FIGS. 13 to 17.

In a further aspect, provided is a chromatography system comprising oneor more cyclonic separators as described above and herein, wherein thechromatography system is pressurized and pumps a supercritical solvent.In varying embodiments, the system comprises 2 to 8 cyclonic separators,e.g., 2, 3, 4, 5, 6, 7 or 8 cyclonic separators. In varying embodiments,the interior of the cyclonic separator is in fluid connection withatmospheric pressure.

In another aspect, provided are methods of performing high pressureseparation and/or extraction procedures using a flash chromatographysystem, comprising separating sample in a supercritical fluid mobilephase in the inner chromatography column of the pressure equalizingvessel as described above and herein.

Cyclonic Separator

In one aspect, provided is a cyclonic separator comprising:

a) a cyclone body comprising an inner surface, an outer circumference, atop outlet, a tangential inlet and a bottom outlet, wherein the innersurface comprises a top portion, a middle portion and a bottom portion,wherein:

i) the top portion of the inner surface comprises screw threads;

ii) the middle portion of the inner surface is cylindrical;

iii) the bottom portion of the inner surface comprises a funnel, whereinthe funnel has an angle in the range of about 30° to about 60°; andwherein the ratio of the diameter of the outer circumference to theinner diameter of the mid-height of the funnel is in the range of about3 to about 4; and

b) a cap comprising a sintered filter and screw threads, wherein thescrew threads of the cap interlock with the screw threads on the innersurface of the top portion of the cyclone body, wherein the cyclonicseparator can withstand pressures of at least about 1000 psi, andwherein the body is in fluid communication with the cap. In varyingembodiments, the bottom outlet of the body is attached to a collectioncontainer, wherein the body is in fluid communication with thecollection container. In some embodiments, the cyclonic separator canwithstand pressures of up to about 10,000 psi, e.g, up to about 5000psi, e.g., up to about 2000 psi, e.g., up to about 1900 psi, 1800 psi,1700 psi, 1600 psi, or 1500 psi. In varying embodiments, the thicknessof the middle portion and the bottom portion of the cyclone body is atleast about 0.30 inches, e.g., at least about 0.31, 0.32, 0.33, 0.34,0.35, 0.36, 0.37, 0.375, 0.38, 0.39, 0.40 inches. In varyingembodiments, the cyclone body is made of a material selected from thegroup consisting of: stainless steel and titanium. In varyingembodiments, the stainless steel comprises an austeniticnickel-chromium-based alloy or a martensitic nickel-chromium-basedalloy. In varying embodiments, the stainless steel comprises less thanabout 0.1 wt. % carbon. In varying embodiments, the stainless steelcomprises at least a 30,000 psi yield strength. In varying embodiments,the stainless steel is selected from the group consisting of AmericanIron and Steel Institute (AISI) TYPE 304 SS, AISI TYPE 316L, INCONEL®alloy 625, INCONEL® alloy 718, AK Steel 17-4 PH®, HASTELLOY® C-22 andHASTELLOY® C-276. In varying embodiments, the stainless steel is anickel-chromium superalloy selected from the group consisting ofINCONEL® alloy 625, INCONEL® alloy 718, HASTELLOY® C-22 and HASTELLOY®C-276. In some embodiments, the inner surface of the cyclone body isconfigured to induce or guide a conical cyclone of fluid flowing in fromthe tangential inlet. In varying embodiments, the inner surface of thecyclone body does not comprise a filter or a porous surface. In varyingembodiments, the inner surface of the cyclone body does not comprise oneor more baffles. In some embodiments, the cyclone body does not comprisemultiple inlets. In some embodiments, the sintered filter within the capcomprises a G-5 porosity grade (1-16 microns pore size). In someembodiments, the funnel has an angle of about 40°; and the ratio of thediameter of the outer circumference to the inner diameter of themid-height of the funnel is about 3.5. In varying embodiments, thebottom outlet remains open. In some embodiments, the cyclonic separatoris as depicted in any one of FIGS. 13 to 17.

In a further aspect, provided is a chromatography system comprising oneor more cyclonic separators as described above and herein, wherein thechromatography system is pressurized and pumps a supercritical solvent.In varying embodiments, the system comprises 2 to 8 cyclonic separators,e.g., 2, 3, 4, 5, 6, 7 or 8 cyclonic separators. In varying embodiments,the interior of the cyclonic separator is in fluid connection withatmospheric pressure.

In varying embodiments, the chromatography system further comprises apressure equalizing vessel upstream of and in fluid communication withthe cyclonic separator, the pressure equalizing vessel comprising:

i) an inner chromatography column comprising stationary phase media; and

ii) an outer column that cylindrically surrounds the length of the innercolumn, wherein the interspace between the inner diameter of the outercolumn and the outer diameter of the inner chromatography columncomprises a width of at least 1 mm, wherein the outer column withstandspressures of at least about 500 psi (about 35 bar), and wherein no partof the inner column is exposed to full internal pressure withoutbalancing external equalizing pressure. In varying embodiments, theinterspace has a width of up to about 2, 3, 4, 5, 6, 7, 8, 9, 10, 11,12, 13, 14, 15, 16, 17, 18, 19 or 20 mm. In varying embodiments of thepressure equalizing vessel, the interspace between the inner diameter ofthe outer column and the outer diameter of the inner chromatographycolumn is filled with a supercritical fluid. In some embodiments, theinner column and the outer column can be concurrently filled withsupercritical fluid under a pressure in the range of about 500 psi(about 35 bar) to about 20,000 psi (about 1380 bar). In someembodiments, the inner column and the outer column can be concurrentlyfilled with supercritical fluid under a pressure in the range of atleast about 5076 psi (at least about 350 bar). In some embodiments, thepressure differential across the inner column from top to bottom is lessthan the pressure rating of the inner column. Generally, the pressuredifferential between the internal space of the inner column and theinterspace is less than the pressure rating of the inner column. In someembodiments, the pressure differential between the internal space of theinner column and the interspace is at or less than about 200 psi (about14 bar). In some embodiments, the pressure within the interspace ishigher than the pressure within the internal space of the inner column.In some embodiments, the inner column comprises an inlet end and anoutlet end and the pressure at the inlet end is substantially the sameas the pressure at the outlet end. In some embodiments, the inner columnis an off-the-shelf column compatible for use in a flash chromatographysystem. In some embodiments, the inner column comprises a size in therange of from about 4 grams to about 350 grams stationary phase media.In some embodiments, the inner column comprises a diameter in the rangeof about 0.5 inches to about 3.5 inches and a column length in the rangefrom about 3.5 inches to about 11 inches. In some embodiments, thestationary phase comprises an average particle size in the range ofabout 10 to about 100 microns, e.g., in the range of about 20 to about80 microns. In some embodiments, the pressure equalizing vesselcomprises an inlet adaptor which fits to a female slip or luer-lockconnector. In some embodiments, the pressure equalizing vessel comprisesan outlet adaptor which fits to a male slip or luer-lock connector. Insome embodiments, the outlet adaptor comprises an 0-ring that sealsaround the male slip or luer-lock connector. In some embodiments, theinner column comprises an inlet end and an outlet end, wherein neitherthe inlet end nor the outlet end of the inner column comprises aperforated stopper. In some embodiments, the interspace comprises asingle inlet and no outlet or vent. In some embodiments, the pressureequalizing column is as depicted in FIGS. 11 and 12.

In varying embodiments, the chromatography system further comprises asupercritical solvent pump and a chiller in fluid communication with andupstream of the pump and the cyclonic separator, wherein the chillerreduces the temperature of the supercritical solvent to about −5° C. orlower, e.g., about −10° C., −15° C., −20° C., −25° C., or lower. In someembodiments, the chiller comprises:

a) a first refrigerant circuit, comprising:

-   -   i) a first compressor that pumps refrigerant through the first        refrigerant circuit;    -   ii) a first tube-in-tube heat exchanger in fluid communication        with the first compressor, wherein the first tube-in-tube heat        exchanger comprises an inner lumen and an outer lumen that        surrounds the inner lumen, wherein the refrigerant flows through        the outer lumen;

b) a cryogenic refrigerant circuit in thermodynamic communication withthe first refrigerant circuit, the cryogenic refrigerant circuitcomprising:

-   -   i) a second compressor that pumps cryogenic refrigerant through        the cryogenic refrigerant circuit;    -   ii) the first tube-in-tube heat exchanger in fluid communication        with the second compressor; wherein the cryogenic refrigerant        flows through the inner lumen;    -   iii) a second tube-in-tube heat exchanger in fluid communication        with the first tube-in-tube heat exchanger; wherein the second        tube-in-tube heat exchanger comprises an inner lumen and an        outer lumen that surrounds the inner lumen, wherein the        cryogenic refrigerant flows through the outer lumen and wherein        liquefied gas or supercritical gas flows through the inner        lumen;

wherein the chiller does not comprise an intervening medium thatmediates heat exchange between the first refrigerant circuit and thecryogenic refrigerant circuit and wherein the liquefied gas orsupercritical gas exiting the inner lumen of the second tube-in-tubeheat exchanger is chilled. In varying embodiments, the output liquefiedgas or supercritical gas is chilled at least about 35° C. lower than theinput liquefied gas or supercritical gas. In varying embodiments, therefrigerant is selected from the group consisting of R-11, R-12, R-22,R-32, R-114, R-115, R-123, R-124, R-125, R-134A, R-142b, R-143a, R-152a,R-290, R-401A, R-401B, R-404A, R-407C, R 410A, R-409A, R-414B, R-416A,R-422B, R-422D, R-500, R-502, R-507, R-600 and mixtures thereof. Invarying embodiments, the cryogenic refrigerant is selected from thegroup consisting of R-12, R-13, R-22, R-23, R-32, R-115, R 116, R-124,R-125, R-134A, R-142b, R-143a, R-152a, R-218, R-290, R-218, R-401A, R401B, R-402A, R-402B, R-403B, R-404A, R-408A, R-409A, R-410A, R-414B,R-416A, R-422B, R-407A, R-407C, R-408A, R-409A, R-414B, R-422A, R-422B,R-422C, R-422D, R-500, R-502, R-503, R-508B, R-507, R-508B, R-600a andmixtures thereof. In varying embodiments, the first refrigerant circuitfurther comprises in fluid communication with the first compressor andthe first tube-in-tube heat exchanger: iii) a first expansion valve; andiv) a liquid to air heat exchanger. In varying embodiments, thecryogenic refrigerant circuit further comprises in fluid communicationwith the second compressor, the first tube-in-tube heat exchanger andthe second tube-in-tube heat exchanger: iv) a second expansion valve. Invarying embodiments, the chiller comprises a configuration as depictedin FIGS. 3A-3B. In some embodiments, the system comprises:

a) a tank comprising a gas stored at saturated conditions and a liquidwithdrawal means;

b) a chiller in fluid communication with the tank, wherein the chillersubcools the gas to a temperature of −10° C. or lower;

c) a pump downstream of and in fluid communication with the tank and thechiller, and a chamber configured for liquefied gas or supercritical gasextraction, wherein the pump comprises the gas at a temperature of −10°C. or lower; wherein the mass flow rate of the subcooled liquid phasegas through the pump is repeatable and proportionate to pump speed. Insome embodiments, the gas is selected from the group consisting ofcarbon dioxide, n-butane, n-propane, isobutane, dimethyl ether, andmixtures thereof. In some embodiments, the pump is a positivedisplacement pump. In some embodiments, the positive displacement pumpis an unmodified high performance liquid chromatography (HPLC) pump. Invarying embodiments, the system further comprises a post-pump heaterdownstream of and in fluid communication with the pump, wherein thepost-pump heater heats the liquefied gas or supercritical gas up to anoperational temperature.

In varying embodiments, the supercritical fluid is CO2. In varyingembodiments, the flow of the supercritical solvent through the system isin the range of about 10 ml/min, e.g., at least about 15 ml/min, 20ml/min, 25 ml/min, 30 ml/min, 35 ml/min, 40 ml/min, 45 ml/min, or 50ml/min, to about 300 ml/min. In varying embodiments, the system furtherpumps a co-solvent. In some embodiments, the co-solvent comprises analcohol of 3 or fewer carbon atoms (e.g., methanol, ethanol, propanol,isopropanol) or an acetate of 3 or fewer carbon atoms (e.g., methylacetate, ethyl acetate, propyl acetate), or mixtures thereof. In varyingembodiments, the system is as depicted in FIG. 1.

In a related aspect, provided are methods of separating molecules from asupercritical fluid. In varying embodiments, the methods compriseinputting a stream of gas phase supercritical fluid comprising moleculesinto the tangential inlet of a cyclonic separator as described above andherein, wherein the stream of supercritical fluid rotates around theinner surface of the cyclone body, wherein the molecules separate fromthe stream, slide down the inner surface and exit the cyclone body intothe collection container; and wherein the gas phase supercritical fluidexits through the cap, and wherein any molecules still in the fluidstream do not escape through the sintered filter of the cap. In varyingembodiments, the interior of the cyclonic separator is in fluidconnection with atmospheric pressure.

Definitions

The phrase “conical cyclone of fluid” refers to a downward spiral pathwhich substantially does not cross itself.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a flow schematic of a chromatography system describedherein.

FIG. 2 illustrates an apparatus schematic of a chromatography systemdescribed herein.

FIGS. 3A-B. FIG. 3A illustrates a block diagram of the chiller's twocircuit cascade refrigeration system. FIG. 3B illustrates the chillerand HPLC pumps package. The post pump heater is used to bring processfluids up to operational temperatures.

FIG. 4 illustrates a plot of mass flow rate vs. temperature at a set RPMof 250.

FIG. 5 illustrates a plot of mass flow rate vs. temperature at a set RPMof 500.

FIG. 6 illustrates a plot of mass flow rate vs. temperature at a set RPMof 750.

FIG. 7 illustrates trend lines for mass flow vs. temperature at the setRPMs of 250, 500 and 750.

FIG. 8 illustrates an assembly drawing of external views of a productionprototype of the chiller. Enclosure (1). Power entry (3). Fan guard(23). Bulkhead union (25).

FIG. 9 illustrates an assembly drawing of internal views of a productionprototype of the chiller. Fan-cooled heat exchanger (2). Tube-in-tubeheat exchanger (5). Sight glass; moisture indicator (12). Sight glass toservice Tee Tube (14). Access valve (15). Service Tee to suction inlettube (16). Capillary tube winding (21). Union elbow with tube fitting(22). Union coupling with tube fitting (24). Cryo compressor suctioninlet tube (27). Liquid gas outlet tube (28). High capacity compressordrive (30). Mounting bracket (31). Drive board—compressor (32). 1.4 CCcompressor (33).

FIG. 10 illustrates an assembly drawing of internal views of aproduction prototype of the chiller. Fan mounting bracket (4). Reducingcoupling (6). Compressor to condensing tube (7). Solder connection;copper fitting (8). 90 degree long elbow solder connection (9).Condenser to sight port tube (10). Copper tube, 45 degree elbow (13). 90degree long elbow solder connection (17). Dryer, liquid line withservice port (18). Down tube—condenser side (26). Liquid gas inlet tube(29). Power supply (34).

FIG. 11 illustrates a cross sectional view of the pressure equalizingvessel showing the outer pressure containment vessel and the innerchromatography cartridge or column. Insets depict the input and outputattachments of the inner chromatography cartridge or column to the outerpressure containment vessel.

FIG. 12 illustrates a cross sectional view of the pressure containmentvessel in the context of its fluid connections with an exemplarychromatography system.

FIG. 13 illustrates an assembly drawing of the system, including abreakdown of the parts and quantities required.

FIG. 14 illustrates a CFD visualization of the streamlines of the gasflow.

FIG. 15 illustrates a manufacturing print of the Collection CycloneBody.

FIG. 16 illustrates a manufacturing print for the Collection CycloneCap.

FIG. 17 illustrates a detailed internal geometry of the CollectionCyclone Assembly.

FIG. 18 illustrates a separation of aceptophenone and methyl parabenusing the chromatography system described herein.

FIG. 19 illustrates a separation of aceptophenone and methyl parabenusing the chromatography system described herein.

FIG. 20 illustrates a separation of benzoic acid and 4-acetamidophenolusing the chromatography system described herein.

FIG. 21 illustrates a separation of ketoprofen and 4-acetamidophenolusing the chromatography system described herein.

DETAILED DESCRIPTION 1. Introduction

Provided are supercritical fluid chromatography systems that enable theseparation cartridges employed in traditional flash chromatographyapplications to be used in conjunction with a liquefied gas orsupercritical fluid dominated solvent system. This facilitates or allowsfor a substantial reduction on the order 80-90% of the organic solventsor a complete elimination of organic solvents in the separation process.Achieving this goal involves implementation of one or more features toenable operating conditions in the range of pressures associated withsubcritical fluids or subcritical fluids, e.g., in a pressure range ofabout 35 bar or higher pressure. These features include a prechillersystem, a pressure equalizing vessel, and a pressurized cyclonicseparator. When used in coordination, these improvements allow forliquefied gas and supercritical fluids to be utilized where only lowpressure liquid solvents could previously been employed. The prechillersystem enables a standard HPLC pump, nominally optimized for operationwith incompressible fluids, to be employed with a liquefied gas orsupercritical fluid. The pressure equalizing vessel enables anoff-the-shelf chromatography cartridge, nominally intended for use withlow pressure liquid solvents, to be used without further alteration in aliquefied gas or supercritical fluid system. The high pressure cyclonicseparator enables product recovery from a high pressure system andserves the purpose of a collection flask in a high pressure system.

2. Supercritical Fluid Chromatography Systems

The chromatography systems described herein are based, in part, on thediscovery and advanced design of traditional flash chromatographytechnology that employs supercritical fluid (e.g., liquid phase CO2) asthe main non-polar solvent in flash chromatography. FIGS. 1 and 2illustrate a supercritical fluid CO2 flash chromatography apparatus. Invarying embodiments, the apparatus has one or more ofprechiller/supercritical fluid (e.g., CO2) pump that allows for theefficient and accurate delivery of liquid-phase supercritical fluid(e.g., CO2) in a supercritical fluid state to the apparatus up to 10,000psi, e.g., up to 5000 psi or 2500 psi and at a flow rate of at leastabout 10 mls/min and up to about 250 ml/min or 300 ml/min, a secondaryco-solvent pumping package that allows for polar modifier solvents(e.g., co-solvents) to be added to the flow stream in an isocratic orgradient mode (2500 psi and 100 mls/min), an injection manifold that cantake the form of an injection loop or a secondary injection column forlarger sample injection, a pressure equalizing vessel assembly thatallows traditional flash column cartridges to be used in the apparatusup to the pressures of operation, a UV-VIS detector (other detectorsoptional), and a back pressure regulator (BPR) upstream of and in fluidcommunication with a stream selector, which is in fluid communicationwith the one or more cyclonic separators. The BPR brings the pressure ofthe flow stream from operation pressures down to ambient pressures forfraction collection in the cyclonic separators.

Generally, the chromatography systems are pressurized to pumpsupercritical fluid (e.g., CO2), with or without co-solvent. In varyingembodiments, the system further pumps a co-solvent. When pumping asupercritical fluid mixed with a co-solvent, the co-solvent may compriseup to about 20% v/v of the fluid being pumped through the system. Asshown in FIG. 1, the co-solvent is delivered through an input pumpseparate from the supercritical fluid input pump, and mixed with thesupercritical fluid prior to delivery to the inner column of thepressure equalizing vessel. In some embodiments, the co-solventcomprises an alcohol of 3 or fewer carbon atoms (e.g., methanol,ethanol, propanol, isopropanol) or an acetate of 3 or fewer carbon atoms(e.g., methyl acetate, ethyl acetate, propyl acetate), or mixturesthereof.

3. Chiller for Pumping Supercritical and Liquified Gases

a. Introduction

A system for super chilling liquid gases (e.g., including carbondioxide, methane, ethane, propane, butane, ethylene, propylene, andethers) and to increase pumping efficiency and consistency is provided.The chiller cools liquid gases (e.g., including carbon dioxide, methane,ethane, propane, butane, ethylene, propylene, and ethers) to between−10° C. and −40° C. has been shown to enable the use of a standard HPLCpump with increased mass flow rates at a constant set point as thetemperature is reduced. The herein described system reduces the cost ofpumping CO2 by allowing the use of traditional HPLC pumps, rather thanhighly specialized CO2 pumps.

The present systems and methods use a cascade chiller to cool the liquidCO2 to less than −10° C., e.g., in varying embodiments, less than −20°C., to minimize the variance in pump performance. The lower temperaturesenable greater tolerance for the flow path in the high pressure CO2 pumphead and facilitate the use of an unmodified HPLC (High Pressure LiquidChromatography Pump). Traditional HPLC pumps are normally intended forpumping liquids; not liquid gases. There is a wide scatter in flowperformance that results when the liquid is chilled to only 0° C. Atroom temperature conditions the variance would be greater than 30% andwould render the unmodified HPLC pump completely ineffective insupercritical chromatography applications. The herein described chillerand methods allows the use of a traditional HPLC for precise meteredpumping of liquid-gases, e.g., for delivery to extractors, reactors andchromatography equipment.

We have determined that extreme subcooling much improved pumpingperformance. The pumping mass flow rate was linearly related to speedand repeatability. In this case, the supercritical CO2 was subcooledfrom an ambient condition of nearly 25° C. and 52 bar to approximately−25° C. and 52 bar. This 55° C. temperature reduction resulted in theliquid CO2 conditions more closely resembling an incompressible fluid,such as water. A completely unmodified and standard HPLC pump can thenbe used to pump the scCO2 under very linear conditions. Such behavior ishighly desirable for applications including supercritical fluidextraction, supercritical fluid solid phase extraction, supercriticalfluid flash chromatography, and supercritical fluid chromatography.

The use of this hook of physics is advantageous in these applications,as it enables standard and cost-effective HPLC pumps to be used insupercritical fluid applications with highly linearly mass flow rateswithout the need for either elaborate compensation algorithms, sensorfeedback systems involving compensation via a loss in weight measurementof the supply cylinder, direct compensation via a mass flow measure(e.g. coriolis mass meter), or the need for a booster pump to stabilizethe delivery flow to the pumping system.

b. Prechiller or Chiller-HPLC Pump Assembly

Generally, the prechiller or chiller utilizes dual refrigerationcircuits with tube-in-tube heat exchangers that allow for heat exchangewithout an intervening heat exchange medium. FIG. 3A illustrates a blockdiagram of the two circuit cascade refrigeration heat exchanger presentin the chiller. The two circuits are a low temperature circuit and ahigh temperature circuit. In such systems, the two circuits arethermally coupled at the condenser of the low temperature circuit. Infact, the condenser of the low temperature circuit is the evaporator ofthe high temperature circuit. To further simplify the concept, the lowtemperature circuit in the chiller is used to super chill the CO2 flowto its target temperature and the high temperature circuit is used toremove the heat from the low temperature circuit.

CO2 flow enters the evaporator of the low temperature circuit at bottlepressure/temperature. Said evaporator is a tube in tube heat exchangerwith an inner tube made of AISI Type 316 stainless steel or similarmetal suitable for exposure to CO2. Other materials of use for the innertube include without limitation copper, brass, and Type 304 stainlesssteel. Heat is removed from the CO2 by the flow of cryogenic refrigerantin the outside tube which is made of copper and surrounds the insidetube. The heat exchanger is set up as a counter flow heat exchanger forgreater efficiency.

The low temperature circuit is used to pull heat from the CO2 flow tochill it to the required temperature. A cryogenic refrigerant enters thesuction side of the compressor and is discharged at a higher pressure.The compressor is a 1.4 CC model by Aspen. Work is done by thecompressor to increase the pressure of the cryogenic refrigerant, whichraises its temperature. The cryogenic refrigerant then exits thecompressor on the discharge (high pressure) side and enters the lowtemperature circuit condenser. The low temperature circuit condenser isthe same unit as the high temperature circuit evaporator. The condenseris a tube in tube heat exchanger. The cryogenic refrigerant flowsthrough the inside tube of the heat exchanger. Heat is removed from thecryogenic refrigerant by a conventional refrigerant flowing in theoutside tube which surrounds the inside tube. This heat exchanger isarranged as a counter flow heat exchanger for greater efficiency. Afterhaving the heat removed the cryogenic refrigerant flows through amoisture indicator, and then a dryer which has a built in service port.This is the high pressure side service port. After the dryer, thecryogenic refrigerant flows through an expansion valve. In this case,the expansion valve is a coiled length of capillary tube. When thecryogenic refrigerant exits the expansion valve, it is returned back toa low pressure state, which reduces the temperature before it enters thelow temperature circuit evaporator. The cryogenic refrigerant flowsthrough the outside tube of the evaporator and removes heat from the CO2flowing through the inside tube which it surrounds. Upon exit, thecryogenic refrigerant flows through a moisture indicator and a servicetee before returning to the suction side of the low temperature circuitcompressor. This cycle is continuous.

The high temperature circuit uses a similar flow path with one majordifference. The condenser of the low temperature circuit is a fan cooledliquid to air heat exchanger. In the high temperature circuit, aconventional refrigerant enters the suction side of the compressor andis discharged at a higher pressure. The change in pressure isaccompanied by a rise in temperature. The refrigerant then flows intothe condenser where forced air is used to remove heat. This heat istransferred to the atmosphere and out of the system. The refrigerantthen flows through a moisture indicator and a dryer with built inservice port before going through the expansion valve. On exit of theexpansion valve the refrigerant is returned to a lower pressure and thuslower temperature. The refrigerant then enters the evaporator. Here therefrigerant for the high temperature circuit absorbs heat from the lowtemperature circuit in a tube in tube heat exchanger. Upon exit therefrigerant goes through a service tee and a moisture indicator beforereturning to the suction side of the compressor. This cycle iscontinuous.

To summarize the two circuit cascade system, it is easiest to follow thetransfer of heat into and then out of the system. In the case of thechiller, heat is brought into the system by a stream of CO2. The removalof heat from the CO2 is the ultimate goal of the system. This heat isremoved by the evaporator of the low temperature circuit. The lowtemperature circuit is then used to transfer heat to the hightemperature circuit. This happens in the high temperature circuitevaporator which is also the low temperature circuit condenser. In thefinal stage of heat transfer, the high temperature circuit transfersheat out of the system and into the atmosphere in the high temperaturecircuit condenser. In short, heat cascades from the CO2 to the lowtemperature circuit then the high temperature circuit and finally theatmosphere.

FIG. 3B illustrates the connection of the chiller to a traditional HPLCtype SCF Pump with the addition of post-pump heaters to bring the fluidsup to operational temperatures.

c. Embodiments of Prechiller or Chiller

In varying embodiments, the chromatography system comprises a prechilleror chiller, as described herein, upstream of a pump to cool thesupercritical fluid sufficiently such that it can be pumped through astandard off-the-shelf, commercially available flash chromatography orhigh performance liquid chromatography (HPLC) pump. The prechillerimproves the pumping performance (e.g., the consistency) for asupercritical fluid, e.g., carbon dioxide such that system mass flowrates are proportionate to pump speed.

In varying embodiments, the prechiller cools the liquid phasesupercritical fluid (e.g., CO2) to a temperature of about −5° C. orless, e.g., −10° C., −15° C., −20° C., −25° C., or less, e.g., but abovethe triple point temperature, e.g., above about −55° C., e.g., to about−40° C., −45° C. or −50° C. Such supercooling or extreme subcoolingreduced in much improved pumping performance. The pumping mass flow ratewas linearly related to speed and repeatability. In varying embodiments,the prechiller subcools the supercritical fluid (e.g., CO2) from anambient condition of nearly 25° C. to approximately −10° C. or lowertemperatures. In varying embodiments, the system employs a 2-stagerefrigerant on refrigerant chiller system to cool and liquefy the gasphase supercritical fluid. In varying embodiments, the system does notdirectly or separately cool the pump heads.

This minimum of 35° C. temperature reduction resulted in thesupercritical fluid (e.g., liquid phase CO2) conditions more closelyresembling an incompressible fluid, such as water. A completelyunmodified and standard HPLC pump can then be used to pump thesupercritical fluid (e.g., liquid phase CO2) under very linearconditions. Such behavior is highly desirable for application includingsupercritical fluid extraction, supercritical fluid solid phaseextraction, supercritical fluid flash chromatography, and supercriticalfluid chromatography.

The supercooling prechiller enables standard and cost effective HPLCpumps to be used in supercritical fluid applications with highlylinearly mass flow rates with the need for either elaborate compensationalgorithms, sensor feedback systems involving compensation via a loss inweight measurement of the supply cylinder, direct compensation via amass flow measure (e.g., coriolis mass meter), or the need for a boosterpump to stabilize the flow.

4. Pressure Equalizing Vessel

a. Introduction

Pressure equalization assemblies and methods of use are provided. Morespecifically, provided is a pressure equalization assembly that enablesthe use of low-medium pressure columns for flash chromatography in ahigher pressure supercritical fluid chromatography application. Thepressure equalization assemblies allows the attachment of commerciallyavailable chromatography columns or cartridges to the cap of the vessel,e.g., via a luer lock fitting, and seals on the other end using anO-ring or gasket that is captured axially by the cap and tapered stem ofsaid column. Sample stream pressure going through the column is balancedby external pressure applied to the same column to maintain a pressuredifferential that is less than the standard operating pressure of thecolumn. In doing so, it ensures that the columns can be used withoutfailure for high pressure supercritical fluid chromatography.

b. Embodiments of the Pressure Equalizing Vessel

In varying embodiments, the supercritical fluid chromatography systemcomprises a pressure equalizing vessel. The pressure equalizing vesselis designed to allow the use of commercially available or off-the-shelflow to medium pressure columns (e.g., in the range of about 14-200 psi)traditionally used in flash chromatography at the higher pressures (inthe range of about 1000 psi to about 10,000 psi, e.g., in the range ofabout 1500-2000 psi) used in Supercritical Flash Chromatography. Thepressure equalizing vessels described herein allow the use of moreeconomical pre-packed disposable columns in Supercritical FlashChromatography, rather than expensive high pressure columns that must bere-packed by the user.

The pressure equalization vessel described herein utilize pressureequalization to allow the low pressure columns to exceed their ratedburst pressures. This is accomplished by pressurizing the outside of thecolumn to a level that ensures that the pressure differential betweenthe flow through the inside of the column and the equalizing pressure onthe outside of the column remains within the rated pressure of thecolumn. For example, if a column is rated at 200 psi normal operatingpressure, and the user desired to run at higher pressure ranges of about1000 psi to about 10,000 psi, e.g., 1500-2000 psi, the system wouldensure that the equalizing pressure is within 200 psi of workingpressure. Testing has proven this to be effective at preventing failureof the columns due to overpressure.

The pressure equalization system allows the attachment of commerciallyavailable or off-the-shelf flash chromatography columns to the cap ofthe vessel via a luer lock fitting, and seals on the other end using anO-ring or gasket that is captured axially by the cap and tapered stem ofsaid column. The pressure equalizing vessel is compatible for use withany commercially available pre-packed flash chromatography cartridge,including without limitation cartridges made by Grace (grace.com),Silicycle (silicycle.com), Biotage (biotage.com), Teledyne-ISCO(isco.com), Buchi (buchi.com), Interchim Inc. (interchiminc.com), andAgilent (agilent.com). The pressure equalizing vessel does not limit thesize of the inner column cartridge that can be used, but is designed toadjust and accommodate to the chromatography cartridge appropriate for adesired separation. In varying embodiments, the inner column can containin the range of from about 4 grams to about 350 grams stationary phasemedia, e.g., 4 grams, 8 grams, 12 grams, 20 grams, 80 grams, 120 gramsor 330 grams stationary phase media. In varying embodiments, the innercolumn comprises a diameter in the range of about 0.5 inches to about3.5 inches and a column length in the range from about 3.5 inches toabout 11 inches. Illustrative diameter and length sizes of the innercolumn include without limitation 0.94 inches diameter×3.85 incheslength (4 grams stationary media); 1.38 inches diameter×4.60 incheslength (12 grams stationary media); 1.77 inches diameter×6.43 incheslength (40 grams stationary media); 1.99 inches diameter×9.50 incheslength (80 grams stationary media); 2.18 inches diameter×10.31 incheslength (120 grams stationary media); or 3.39 inches diameter×10.55inches length (330 grams stationary media).

Sample stream pressure going through the column is balanced by externalpressure applied to the same column to maintain a pressure differentialthat is less than the standard operating pressure of the column. Indoing so, it ensures that the columns can be used without failure forhigh pressure supercritical fluid chromatography.

FIG. 11 illustrates a cross sectional view of the system. It shows thepressure containment vessel, the medium pressure column, and the methodsfor attaching the column to the vessel itself. The fittings of thepressure equalizing vessel can be readily adjusted to accommodate theinner column being used, wherein the standard input fitting accommodatesa female luer lock on the inner column and the standard output fittingaccommodates a male slip fitting on the inner column. In the embodimentdepicted in FIG. 11, a luer lock connection provided on thesupercritical fluid (e.g., CO2) plus optional co-solvent inlet of thecolumn seals the outside pressure from the sample stream pressure. Theluer lock adapter is shown as a threaded adapter in this print, but mayalso be an integral machined part of the vessel cap, or also a weldedadapter. On the other end of the column, the outside equalizingpressure, and the sample stream pressure are sealed from each otherusing an O-ring or gasket, on the outside of the column stem. The cap ofthe vessel has a shelf to capture said gasket and the column stem istapered so that it also helps capture the gasket in position byproviding an axial force. This tapered stem and the luer lock on theopposite end are typical of industry standard low-medium pressurecolumns.

FIG. 11 also shows the inlet connection for the sample stream. Thisstream typically is composed of a supercritical fluid (e.g., CO2),optionally a co-solvent, and the sample to be separated. The fittingshown is a high pressure compression fitting made to seal on the outsidediameter of appropriately sized high pressure tubing. The same type offitting is used for the Sample stream outlet, and the pressureequalizing inlet. The pressure equalizing medium will typically be asupercritical fluid (e.g., CO2).

FIG. 12 illustrates a cross sectional view of an example supercriticalflash chromatography system with the pressure equalization systemincorporated. FIG. 12 illustrates the typical inputs of supercriticalfluid (e.g., CO2) and co-solvent, and shows how the system equalizespressure in this case. Input flow of supercritical fluid (e.g., CO2) issplit, one direction serves as the pressure equalizing fluid, and theother direction is used in conjunction with co-solvent to flow with thesample through the column. The system pressure is controlled by a backpressure regulator.

The check valve after the input tee for supercritical fluid (e.g., CO2)ensures that the pressure is typically greater on the outside of the lowpressure column. This means that if any leaks were to occur, the leakswould occur from outside equalizing fluid, into the column. Thisprotects the valuable samples being separated from being lost.

5. Cyclonic Separator

a. Introduction

In varying embodiments, the supercritical fluid chromatography systemcomprises a cyclonic separator. The cyclonic separator is designed toefficiently and effectively separate sample molecules from a liquidphase or gas phase stream of a supercritical fluid, e.g., CO2. Theseparator is designed to accept tangential input flow, e.g., via tubecompression fitting, allowing the separator to accept typical industrystandard tubing. Using a tangential inlet, the flow is channeled in acyclonic flow around the separator to separate the molecules from thegaseous flow by centrifugal force. The separator deposits the samplemolecules conveniently into an attached sample collection jar, and canbe completely disassembled for complete cleaning. To ensure anymolecules not successfully separated by the centrifugal forces of thecyclone are not released to atmosphere, a sintered filter of anappropriate size (e.g. having a porosity grade of G-5, or a pore size inthe range of about 1-16 microns) can be pressed into the exit of thecyclone, allowing only the gaseous flow to escape.

b. Embodiments of the Cyclonic Separator

The herein described cyclonic separators are designed to separatemolecules from a gas phase supercritical fluid (e.g., CO2) flow andcollect the molecules in a sample jar. In varying embodiments,separation procedures are performed at flow rates in the range of about10-300 ml/min, e.g., about 250 ml/min, and at pressures in the range ofabout 1000-10,000 psi, e.g., about 1500-2000 psi or about 1,750 psi. Thecyclonic separators can be used within a pressurized chromatographysystem and in fluid communication with a sample stream using compressionfitting adapters and can be vented to atmosphere directly, or by hookingup a hose to the outlet. All materials of construction are suitable foruse with corrosive solvents.

Other forms of cyclonic separators have been used in the past to attemptto separate a desired sample from CO2/co-solvent streams in thesupercritical fluid extraction products. These have been much cruder,simpler devices typically consisting of an inlet tube that would bringthe fluid/particle stream into a collection vessel at 90 degrees, theproduct stream would circulate around the interior diameter of thecollection vessel and the particulate products and modifier co-solventswould drop out and settle at the bottom of the collection assembly andthe gaseous SCF CO2 would vent through and an outlet tube. The problemwith these devices was always the loss of desired product to the fluidgaseous stream on the outlet. This was because none of the devices weredesigned to form a true cyclonic flow, nor were they equipped withproper filtration on the outlets. By contrast, with the presentlydescribed cyclonic separators, a cyclonic flow path is induced in whichthe gas is forced into rotational flow around the exit tube facilitatedby the tangential inlet, and is then forced into a downward spiral intowards the low pressure region by the conical section. The low pressureregion is in the middle of the volume where the exit is located.

FIG. 13 illustrates an overall assembly drawing of the cyclonicseparator and collection assembly. The cyclone body is connected to thefluid stream using a National Pipe Thread (NPT)×compression adapter. Inthis illustrated assembly, the compression fitting is sized for ⅛″ tubeand the NPT fitting is 1/16″. Compression fittings sized in the range ofabout 1/16 inches to about ¼ inches find use. The cyclone cap threadsinto the top of the cyclone body and seals against an O-ring. Thisensures that pressure is not lost through the threads. The cap has asintered filter pressed into the exit to ensure that any samplemolecules that may not have been separated by the vortex flow arecaptured and not released to atmosphere. Pore sizes of the sintered disccan be sized for particular compounds. In the illustrated iteration,sintered filter having a porosity grade G-5 is used (1-16 microns poresize). In varying embodiments, sintered filters with G-0 to G-5 porositygrade find use (G5=pore size in the range of about 1-16 microns; G4=poresize in the range of about 10-16; G3=pore size in the range of about16-40 microns; G2=pore size in the range of about 40-100 microns;G1=100-160 microns; and G0=pore size in the range of about 160-250microns).

The cyclone body can be configured to be adapted to many standardcollection jars. In the embodiment illustrated in FIG. 13, a 500 mLglass collection jar is used. The cyclone body can have a threadedbottom exit for attachment and sealing to the collection jar. The cap ofthe jar can have a through hole, which allows the cyclone body to besecured to the cap using a nut. This connection can be sealed using anO-ring, as illustrated.

FIG. 14 illustrates the result of a Computational Fluid Dynamics (CFD)streamline study done to optimize the geometry of the cyclone at 250mL/min @1,750 psi of supercritical CO2 flow. When the CO2 flow reachesthe cyclone, it is no longer at such high pressures because the cycloneis open to atmospheric pressure. Because of this, the mass flow rate wascalculated and then used to determine the velocity of the streamentering the cyclone. The shapes utilized have been done so to properlyfunction with the parameters of the particular CFD program. Though theappearance may differ slightly from the assembly in FIG. 13, theinternal geometry of the cyclone body is the same. The stream linespictured illustrate the path and velocity of the fluid flow. The colorsvary from red to blue, with red indicating the highest stream velocity,and blue indicating the lowest stream velocity. Most importantly, FIG.14 illustrates the downward spiral, substantially non-overlapping streamlines typical of an optimized cyclonic separator.

As illustrated in FIG. 14, flow enters the cyclone body tangential tothe inside diameter. The flow then begins to rotate around the exit tubeof the cyclone. The centrifugal forces exerted on the molecules in thestream lines send the molecules outwards to the wall of the cyclonebody, where a boundary layer keeps the streamlines from recollecting themolecules. The molecules are then free to fall to the bottom of thecollection assembly. As the stream lines travel to the bottom of thecyclone body and hit the conical section, the velocity slows and thepressure increases. This forces the streamlines up the exit tube whichis a low pressure escape from the higher pressure conical section.

FIG. 15 illustrates the manufacturing print released to the machine shopfor the current revision of the cyclone body. All dimensions andinformation pertinent to the manufacturing of the part are present. Inthe illustrated embodiment, the threads used to secure the cap to thebody are the 1″-24 Class 2-B threads. Thread size is determined by thebody of the cyclone, wherein the thread size and conformation areselected to withstand pressure and secure the cap. Generally, thethreads are larger than the inside diameter of the cyclone body. In theillustrated embodiment, the body is secured to the collection vesselusing a ⅜″-32 National Extra Fine (NEF) thread. The function of thecyclone is not dependent on these threads, they were selected to aid inmanufacturing and assembly.

FIG. 16 illustrates configurations of the cyclone cap. In theillustrated embodiment, the cyclone cap is secured to the cyclone bodyvia screw threads. The ledge at the top the cap allows for a sinteredfilter to be pressed into the cap.

FIG. 17 illustrates the internal dimensions of the cyclone. Thesedimensions were honed by using CFD visualization of streamlines, asillustrated in FIG. 14. Dimensions important to the functionalityinclude the ratio of the diameter of the outer circumference to theinner diameter of the mid-height of the funnel in the range of about 3to about 4, e.g., about 3.5. In varying embodiments, the funnel has anangle in the range of about 30° to about 60°, e.g., in the range ofabout 35° to about 55°, e.g., an angle of about 30°, 35°, 40°, 45°, 50°,55°, 60°. The illustrated embodiment depicts a 0.875 diameter to 0.250diameter ratio (e.g., a ratio of 3.5) along with a 40 degree funnelangle. A further important dimension includes the dimensions of theprotrusion at the bottom of the cap. Generally, the depth of protrusionat the bottom of the cap extends below the tangential inlet In varyingembodiments, the depth of protrusion at the bottom of the cap extends,e.g., in the range of about 0.5 inches to about 1 inch, e.g., in therange of about, 0.6 inches to about 0.9 inches, e.g., about 0.50, 0.55,0.60, 0.65, 0.70, 0.75, 0.80, 0.85, 0.90, 0.95 or 1.0 inches. This zonerepresents a part of the internal geometry of the cyclone collectionassembly (see, FIG. 16).

6. Methods of Separating Molecules

Further provided are methods of performing high pressure separationand/or extraction procedures using a flash chromatography system,comprising employing the chiller or prechiller, as described above andherein. The chromatography systems comprising a pressure equalizingvessel, as described herein, are useful for the separation of moleculesthat can be separated using liquid chromatography, e.g., flashchromatography employing commercially available off-the-shelf columncartridges and off-the-shelf HPLC positive displacement pumps.Generally, molecules that can be successfully separated when employing asupercritical fluid solvent have a higher density than the supercriticalsolvent, for example, the molecules may have a higher density thansupercritical, liquid phase and/or gas phase supercritical fluid (e.g.,CO2). In varying embodiments, the molecules to be separated in thepresently described chromatography systems comprising a cyclonicseparator are small organic compounds, peptides, polypeptides, lipids,carbohydrates, nucleic acids and/or polynucleotides. In varyingembodiments, the molecules to be separated can have a molecular weightin the range of about 40 daltons (Da or 40 gram/mol) to about 1,000,000Da (g/mol), or more, e.g., in the range of about 100 Da (g/mol) to about10,000 Da (g/mol), e.g., in the range of about 100 Da (g/mol) to about5,000 Da (g/mol).

In varying embodiments, the methods entail inputting a sample to beseparated that is dissolved or suspended in a supercritical fluid (e.g.,CO2), with or without co-solvent, into the inner column of the pressureequalizing vessel assembly. In varying embodiments, separationprocedures are performed at flow rates in the range of about 10-300ml/min, e.g., about 250 ml/min, and at pressures in the range of about1000-10,000 psi, e.g., about 1500-2000 psi or about 1,750 psi. Theinterspace of the pressure equalizing vessel surrounding the innercolumn is also filled with supercritical fluid at a pressure such thatthe pressure differential between the pressure within the interspace andthe pressure within the inner space of the inside column is less thanthe pressure rating of the inner column (e.g., less than about 14-200psi). Molecules in the sample are separated according to well-knownprinciples of liquid chromatography using commercially available andoff-the-shelf flash chromatography cartridges or columns packed withsolid phase media commonly used in the art.

EXAMPLES

The following examples are offered to illustrate, but not to limit theclaimed invention.

Example 1 Mass Flow Rates Vs. Temperature Employing the Chiller

FIG. 4 illustrates test data for mass flow rate vs. temperature at 250rpm pump speed. The data is focused around the temperature of −10° C.,where pumping consistency increases and mass flow rate and pumpingefficiency also begin to increase with decreasing temperatures. At anaverage temperature of 0.3° C., average mass flow rate was 0.0433 kg/minwith a standard deviation of 0.0024. At an average temperature of −7.95°C., average mass flow rate was 0.0447 kg/min with a standard deviationof 0.0030. At an average temperature of −14.75° C., average mass flowrate was 0.0487 kg/min with a standard deviation of 0.0018. At anaverage temperature of −23.53° C., average mass flow rate was 0.0525kg/min with a standard deviation of 0.0004. At an average temperature of−30.78° C., average mass flow rate was 0.0546 kg/min with a standarddeviation of 0.0005. All tests were performed at a constant RPM of 250,with a target pressure of 2,000 psi and set point flow rate of 13mL/min. The data shows a trend of increasing mass flow rate below −10°C. and decreased variation.

FIG. 5 illustrates test data for mass flow rate vs. temperature at 500rpm pump speed. The data is focused around the temperature of −10° C.,where pumping consistency increases and mass flow rate and pumpingefficiency also begin to increase with decreasing temperatures. At anaverage temperature of 1.3° C., average mass flow rate was 0.0847 kg/minwith a standard deviation of 0.0104. At an average temperature of −9.23°C., average mass flow rate was 0.1067 kg/min with a standard deviationof 0.0047. At an average temperature of −17.88° C., average mass flowrate was 0.1113 kg/min with a standard deviation of 0.0069. At anaverage temperature of −25.28° C., average mass flow rate was 0.125kg/min with a standard deviation of 0.0005. At an average temperature of−30.37° C., average mass flow rate was 0.132 kg/min with a standarddeviation of 0.0005. All tests were performed at a constant RPM of 500,with a target pressure of 2,000 psi and set point flow rate of 33mL/min. The data shows a trend of increasing mass flow rate below −10°C. and decreased variation.

FIG. 6 illustrates test data for mass flow rate vs. temperature at 750rpm pump speed. The data is focused around the temperature of −10° C.,where pumping consistency increases and mass flow rate and pumpingefficiency also begin to increase with decreasing temperatures. At anaverage temperature of −0.13° C., average mass flow rate was 0.158kg/min with a standard deviation of 0.003. At an average temperature of−8.1° C., average mass flow rate was 0.173 kg/min with a standarddeviation of 0.0047. At an average temperature of −16.2° C., averagemass flow rate was 0.181 kg/min with a standard deviation of 0.001. Atan average temperature of −23.87° C., average mass flow rate was 0.192kg/min with a standard deviation of 0.001. At an average temperature of−31.65° C., average mass flow rate was 0.201 kg/min with a standarddeviation of 0.0004. All tests were performed at a constant RPM of 750,with a target pressure of 2,000 psi and set point flow rate of 70mL/min. The data shows a trend of increasing mass flow rate below −10°C. and decreased variation.

Example 2 Separation of Aceptophenone and Methyl Paraben

0.1 grams of Aceptophenone and 0.1 grams of Methyl Paraben weredissolved in 2 mls of Ethyl Acetate. This sample was injected into thesample loop of the SCF CO2 Flash Chromatography unit with a flow rate of50 mls/minute of SCF CO2 and 10 mls/min of Ethyl Acetate at 1750 psi(120 Bar) and 50° C. These materials were separated through the 40 gramsilica cartridge column and collected in cyclonic separators with a99%+efficiency.

The SCF CO2 Flash unit, for the purposes of the present and followingexamples, was operated at 50 mls/minute SCF CO2 and 10 mls/minute up to17.5 mls/minute of modifier co-solvent in an isocratic or gradient modeat 1750 psi (120 bar) and 50° C. The SCF CO2 Flash Chromatography unitis capable of operation up to 2500 psi (175 bar) with a SCF CO2 flowrate of 250 mls/minute and co-solvent modifier flow rate of up to 100mls/minute with a maximum operational temperature of 100° C. TheUltra-Chiller cools the CO2 liquid coming from the supply tank fromambient temperature down to −25° C. to −30° C. which allows forefficient and accurate pumping of the SCF CO2. Once the SCO2 liquid hasbeen pumped, it flows through a pre heater that brings the fluid fromthe −25° C. to −30° C. pump exit temperature up to operationtemperatures of up to 100° C. The fluid streams (a supercritical fluid,e.g., supercritical CO2, and Co-Solvent modifier) flow through a staticmixer that ensures the homogeneous mixing of the fluids for delivery tothe column assembly. Sample introduction into the unit occurs in twomodes: samples dissolved in solvent up to 5 mls in size are introducedthrough a sample injection loop, larger samples can be introducedthrough a column injection manifold (reaction mixture is evaporated ontoa course silica gel that is placed in the column assembly forinjection).

For the purposes of this work a 40 gram W. R. Grace traditional flashcartridge was used (Grace Reveleris Silica 40 micron, 40 gram, Lot#09071032, P/N 5146132, Pressure Rating 200 psi). However, the pressureequalizing vessel or Column Cartridge Containment Assembly canaccommodate traditional flash cartridges from Grace (4 grams up to 330grams in size) and flash cartridges from other flash chromatographyvendors (Silicycle (silicycle.com), Biotage (biotage.com), Teledyne-ISCO(isco.com), Buchi (buchi.com), etc). The UV-Vis detector was set to 254nm to detect the fractions coming from the separation column to then becollected in the Cyclonic Separator Assemblies. Each individual peak canbe collected as a pure fraction. The results are shown in FIG. 18.

Example 3 Separation of Aceptophenone and Methyl Paraben

0.1 grams of Aceptophenone and 0.1 grams of Methyl Paraben weredissolved in 2 mls of Ethyl Acetate. This sample was injected into thesample loop of the SCF CO2 Flash Chromatography unit with a flow rate of50 mls/minute of SCF CO2 and gradient of 10 mls/min to 17.5 mls/min ofEthyl Acetate at 1750 psi (120 Bar) and 50° C. These materials wereseparated through the 40 gram silica cartridge column and collected incyclonic separators with a 99%+efficiency. The results are shown in FIG.19.

Example 4 Separation of Benzoic Acid and 4-Acetamidophenol

0.1 grams of benzoic acid and 0.1 grams of 4-acetamidophenol weredissolved in 2 mls of Methanol. This sample was injected into the sampleloop of the SCF CO2 Flash Chromatography unit with a flow rate of 50mls/minute of SCF CO2 and gradient of 10 mls/min to 17.5 mls/min ofMethanol at 1750 psi (120 Bar) and 50° C. These materials were separatedthrough the 40 gram silica cartridge column and collected in cyclonicseparators with a 99%+efficiency. The results are shown in FIG. 20.

Example 5 Separation of Ketoprofen and 4-Acetamidophenol

0.1 grams of ketoprofen and 0.1 grams of 4-acetamidophenol weredissolved in 2 mls of Methanol. This sample was injected into the sampleloop of the SCF CO2 Flash Chromatography unit with a flow rate of 50mls/minute of SCF CO2 and gradient of 10 mls/min to 17.5 mls/min ofMethanol at 1750 psi (120 Bar) and 50° C. These materials were separatedthrough the 40 gram silica cartridge column and collected in cyclonicseparators with a 99%+efficiency. The results are shown in FIG. 21.

It is understood that the examples and embodiments described herein arefor illustrative purposes only and that various modifications or changesin light thereof will be suggested to persons skilled in the art and areto be included within the spirit and purview of this application andscope of the appended claims. All publications, patents, and patentapplications cited herein are hereby incorporated by reference in theirentirety for all purposes.

What is claimed is:
 1. A pressure equalizing chromatography vessel for asupercritical fluid chromatography system, said vessel comprising: i) aninner chromatography column having an outer wall extending latitudinallywith an outer diameter and the outer wall extending longitudinally witha length, the inner chromatography column comprising stationary phasemedia; and ii) an outer column that cylindrically surrounds the lengthof the inner chromatography column, wherein an interspace void regionexists between the inner diameter of the outer column and the outerdiameter of the outer wall of the inner chromatography column such thatthe interspace extends the length of the outer wall of the innerchromatography column and comprises a width of at least 1 mm, whereinthe outer column withstands pressures of at least about 500 psi (about35 bar), wherein no part of the inner chromatography column is exposedto an interior-to-exterior pressure differential greater than about 200psi (about 14 bar); wherein the inner chromatography column is apre-packed disposable plastic cartridge compatible for use in a flashchromatography system; and wherein there is no fluid communicationbetween the interspace and the interior of the inner chromatographycolumn.
 2. The pressure equalizing vessel of claim 1, wherein theinterspace between the inner diameter of the outer column and the outerdiameter of the inner chromatography column is filled with asupercritical fluid under a pressure in the range of about 500 psi(about 35 bar) to about 20,000 psi (about 1380 bar).
 3. The pressureequalizing vessel of claim 2, wherein the inner chromatography columnand the outer column can be concurrently filled with supercritical fluidunder a pressure of at least about 1000 psi (about 69 bar).
 4. Thepressure equalizing vessel of claim 3, wherein the inner chromatographycolumn and the outer column can be concurrently filled withsupercritical fluid under a pressure of at least about 5076 psi (atleast about 350 bar).
 5. The pressure equalizing vessel of claim 1,wherein the inner chromatography column is configured to withstandpressures no greater than about 200 psi (14 bar).
 6. The pressureequalizing vessel of claim 1, wherein the pressure differential betweenthe internal space of the inner chromatography column and the interspaceis at or less than about 14 psi (about 1 bar).
 7. The pressureequalizing vessel of claim 1, wherein the pressure within the interspaceis higher than the pressure within the internal space of the innerchromatography column.
 8. The pressure equalizing vessel of claim 1,wherein the inner chromatography column comprises an inlet end and anoutlet end and the pressure at the inlet end is substantially the sameas the pressure at the outlet end.
 9. The pressure equalizing vessel ofclaim 1, wherein the inner chromatography column comprises a capacitysize in the range of from about 4 grams to about 350 grams stationaryphase media.
 10. The pressure equalizing vessel of claim 1, wherein theinner chromatography column comprises a diameter in the range of about0.5 inches to about 3.5 inches and a column length in the range fromabout 3.5 inches to about 11 inches.
 11. The pressure equalizing vesselof claim 1, wherein the stationary phase media comprises an averageparticle size in the range of about 10 to about 100 microns.
 12. Thepressure equalizing vessel of claim 1, wherein the vessel comprises aninlet adaptor which fits to a female slip or luer-lock connector. 13.The pressure equalizing vessel of claim 1, wherein the vessel comprisesan outlet adaptor which fits to a male slip or luer-lock connector. 14.The pressure equalizing vessel of claim 13, wherein the outlet adaptorcomprises an O-ring that seals around the male slip or luer-lockconnector.
 15. The pressure equalizing vessel of claim 1, wherein theinner chromatography column comprises an inlet end and an outlet end,wherein neither the inlet end nor the outlet end of the inner columncomprises a perforated stopper.
 16. The pressure equalizing vessel ofclaim 1, wherein the interspace comprises a single inlet and no outletor vent.
 17. A chromatography system comprising the pressure equalizingchromatography vessel of claim 1, wherein the system is configured to bepressurized and pump a supercritical solvent through the system at aflow rate in the range of about 10 ml/min to about 300 ml/min.
 18. Thesystem of claim 17, wherein the system further pumps a co-solvent.
 19. Amethod of performing high pressure separation and/or extractionprocedures using a flash chromatography system, comprising separatingsample in a supercritical fluid mobile phase in the inner chromatographycolumn of the pressure equalizing chromatography vessel of claim 1.